A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517053



Internal ID15097660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24224894..24386936hg38UCSC Ensembl
Innerchr7:24264513..24426555hg19UCSC Ensembl
Innerchr7:24231038..24393080hg18UCSC Ensembl
Innerchr7:24037753..24199795hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38162043
hg19162043
hg18162043
hg17162043
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670496, nssv674426, nssv674069, nssv692600, nssv653693, nssv652642, nssv687461, nssv695539
Samples
Known GenesNPY
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517053
Frequency
Sample Size2026
Observed Gain3
Observed Loss5
Observed Complex0
Frequencyn/a


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